Benzene, 1-propenyl-

• Formula: C₉H₁₀
• Molecular weight: 118.1757
• IUPAC Standard InChI: InChI=1S/C9H10/c1-2-6-9-7-4-3-5-8-9/h2-8H,1H3 Copy

  
• IUPAC Standard InChIKey: QROGIFZRVHSFLM-UHFFFAOYSA-N Copy
• CAS Registry Number: 637-50-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • (Z)-1-Phenylpropene
  • trans-β-Methylstyrene
• Other names: Benzene, propenyl-; β-Methylstyrene; β-Methylstyrol; ω-Methylstyrene; Isoallylbenzene; Propenylbenzene; 1-Phenyl-1-propene; 1-Phenylpropene; 1-Propene, 1-phenyl-; 1-Propenylbenzene; NSC 65591
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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Normal boiling point

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Levi and Nicholls, 1958
Levi, L.; Nicholls, R.V.V., Formation of Styrene by Pyrolysis of Aromatic Heterocyclic Aldehyde- Aliphatic Acid Anhydride Mixtures on Morden Bentonite, Ind. Eng. Chem., 1958, 50, 1005. [all data]

De Wolfe, Hagmann, et al., 1957
De Wolfe, R.H.; Hagmann, D.L.; Young, W.G., Allylic Rearrangements XXXVII. The Ultraviolet Absorption Spectra of Cinnamylmagnesium Bromide and Dicinnamylmagnesium, J. Am. Chem. Soc., 1957, 79, 4795. [all data]

Gero, 1951
Gero, A., J. Org. Chem., 1951, 16, 1731. [all data]

Levina, 1939
Levina, R.Ya., Zh. Obshch. Khim., 1939, 9, 2287. [all data]

Levy and Dvoleitzska-Gombinska, 1931
Levy, J.; Dvoleitzska-Gombinska, Affinity Capacities and Migration Tendencies XI. Comparison of the Affinity Capacities of Aryl and Alkyl Radicals, Bull. Soc. Chim. Fr., 1931, 49, 1765-6. [all data]

Lespieau, 1930
Lespieau, R., Phenyltrimethylene, C. R. Hebd. Seances Acad. Sci., 1930, 190, 1129-31. [all data]

Boeseken and Blumberger, 1925
Boeseken, J.; Blumberger, J.S.P., Observation on the Speed of Oxidation of Several Aromatic Derivatives of Ethylene by the Prileshajew Reaction, Recl. Trav. Chim. Pays-Bas, 1925, 44, 90. [all data]

Tiffeneau, 1904
Tiffeneau, M., Synthesis of Estragol and of ITs Unsaturated Aromatic Derivatives, C. R. Hebd. Seances Acad. Sci., 1904, 139, 481. [all data]

Perkin, 1896
Perkin, W.H., LXIX. On Magnetic Rotatory Power, especially of Aromatic Compounds, J. Chem. Soc., 1896, 69, 1025-1257. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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